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M Wolter-Roessler

Showing results (1-10 of 5) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|August 14, 2010
[Implantation of multifocal add-on IOLs simultaneously with cataract surgery: results of a prospective study]M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde|December 17, 2008
[Correction of aphakia with retroiridally fixated IOL]M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde|December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology|November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findingsC Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Klinische Monatsblatter Fur Augenheilkunde|August 14, 2010
[Implantation of multifocal add-on IOLs simultaneously with cataract surgery: results of a prospective study]M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde|December 17, 2008
[Correction of aphakia with retroiridally fixated IOL]M Wolter-Roessler, M Küchle
Klinische Monatsblatter Fur Augenheilkunde|December 29, 2005
[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?]C Grünauer-Kloevekorn, S Bräutigam, M Wolter-Roessler, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 26, 2006
[Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy]C Grünauer-Kloevekorn, S Braeutigam, E Weidle, et al.
The British Journal of Ophthalmology|November 13, 2008
TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findingsC Gruenauer-Kloevekorn, I Clausen, E Weidle, et al.
Pageof 1